The aim is to compare three medicines of which any one will be given to patient after surgery intraperitonealy to reduce pain , we shall then note pain level using a scoring method and their dose and time of administration.
Phase 4
- Conditions
- Health Condition 1: K800- Calculus of gallbladder with acutecholecystitis
- Registration Number
- CTRI/2024/01/061044
- Lead Sponsor
- SGT medical college hospital and research institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of either sex of ASA (American Society of Anaesthesiologists) grade I and II of 18-65 years for undergoing laparoscopic cholecystectomy.
Exclusion Criteria
Patients of ASA grade III, IV and V with presence of any psychiatric illness, heart disease, renal impairment and those with an allergy to any of the study drugs will be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The ultimate vision is to improve post operative pain management to the point where pain after surgery can be prevented and managed most effectively.Timepoint: Postoperative pain will be assessed on arrival, 30 minutes, 1 hour, 2 hours, 6 hours and 24 hours.
- Secondary Outcome Measures
Name Time Method 1. To study the effect of intraperitoneal magnesium sulphate on post operative pain based on visual analogue scoring. <br/ ><br>2. To study the effect of intraperitoneal bupivacaine on post operative pain based on visual analogue scoring. <br/ ><br>3. To study the effect of intraperitoneal magnesium sulphate and bupivacaine combination on post operative pain based on visual analogue scoring. <br/ ><br>4. To compare the time for first rescue analgesia and total consumption of the rescue analgesic tramadol during the first postoperative day with all the three modes as above.Timepoint: <br/ ><br>1 year